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首页> 外文期刊>High Energy Chemistry >Femtosecond Dynamics of Excited-State Intramolecular Proton Transfer in o-Tosylaminobenzoic and o-Acetylaminobenzoic Acids
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Femtosecond Dynamics of Excited-State Intramolecular Proton Transfer in o-Tosylaminobenzoic and o-Acetylaminobenzoic Acids

机译:在邻甲苯磺酰基氨基苯甲酸和邻乙酰氨基苯甲酸中激发态分子内质子转移的飞秒动力学

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摘要

The dynamics of excited-state intramolecular proton transfer (ESIPT) and of relaxation processes in o-tosylaminobenzoic acid (TAC) and o-acetylaminobenzoic acid (AAC) have been studied by femtosecond absorption spectroscopy with a time resolution of 30 fs. The ESIPT characteristic time in the TAC dimer and monomer and in AAC monomer is 50 fs. The excited product of photoinduced proton transfer in the mono-mer undergoes effective radiationless deactivation with a characteristic time of 30 ps, one of the channels of which is internal rotation followed by intersystem crossing and internal conversion. The product of ESIPT in the TAC dimer deactivates preferentially into the ground state via radiative transition with a time of 291 ps.ESIPT in the AAC dimer is thermodynamically unfavorable and occurs with a low yield.
机译:飞秒吸收光谱法研究了激发态分子内质子转移(ESIPT)和邻甲苯磺酰基氨基苯甲酸(TAC)和邻乙酰氨基苯甲酸(AAC)中弛豫过程的动力学,其时间分辨率为30 fs。 TAC二聚体和单体以及AAC单体中的ESIPT特征时间为50 fs。单体中光诱导质子转移的激发产物以30 ps的特征时间经历有效的无辐射失活,其通道之一是内部旋转,然后进行系统间交叉和内部转换。 TAC二聚体中的ESIPT产物通过291 ps的辐射跃迁优先失活为基态.AAC二聚体中的ESIPT在热力学上不利,且收率低。

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